Canonical Allele Identifier: CA2580600339

Gene: CPT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68835689C= , CM000673.2:g.68835689C=	GRCh38
NC_000011.9:g.68603157C= , CM000673.1:g.68603157C=	GRCh37
NC_000011.8:g.68359733C=	NCBI36
NG_011801.1:g.11243G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001876.4:c.-14+6086G= MANE Select	NP_001867.2:n.-14+6086G=
ENST00000265641.10:c.-14+6086G= MANE Select	ENSP00000265641.4:n.-14+6086G=
NM_001031847.2:c.-14+6086G=	NP_001027017.1:n.-14+6086G=
NM_001031847.3:c.-14+6086G=	NP_001027017.1:n.-14+6086G=
NM_001876.3:c.-14+6086G=	NP_001867.2:n.-14+6086G=
ENST00000265641.9:c.-14+6086G=	ENSP00000265641.4:n.-14+6086G=
ENST00000376618.6:c.-14+6086G=	ENSP00000365803.2:n.-14+6086G=
ENST00000561996.1:c.-14+8456G=	ENSP00000457663.1:n.-14+8456G=
ENST00000569129.5:c.-14+3863G=	ENSP00000455116.1:n.-14+3863G=
XM_005273762.1:c.83+3863G=	XP_005273819.1:n.83+3863G=
XM_005273762.3:c.83+3863G=	XP_005273819.1:n.83+3863G=
XM_005273763.1:c.83+3863G=	XP_005273820.1:n.83+3863G=
XM_017017220.1:c.-14+8456G=	XP_016872709.1:n.-14+8456G=